Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g08950 A05 4474879 C T upstream_gene_variant MODIFIER c.-1904C>T| S293
2 BAA05g08950 A05 4475431 C T upstream_gene_variant MODIFIER c.-1352C>T| S17
3 BAA05g08950 A05 4475956 G A upstream_gene_variant MODIFIER c.-827G>A| S216
4 BAA05g08950 A05 4476807 G A missense_variant MODERATE c.25G>A|p.Asp9Asn S262
5 BAA05g08950 A05 4476902 G A synonymous_variant LOW c.120G>A|p.Pro40Pro S133
6 BAA05g08950 A05 4476986 G A synonymous_variant LOW c.204G>A|p.Arg68Arg S174
S265
S27
S39
7 BAA05g08950 A05 4476989 C T splice_region_variant&synonymous_variant LOW c.207C>T|p.Ile69Ile S204
8 BAA05g08950 A05 4478082 C T synonymous_variant LOW c.652C>T|p.Leu218Leu S65
9 BAA05g08950 A05 4478122 C T missense_variant MODERATE c.692C>T|p.Pro231Leu S79
S84
10 BAA05g08950 A05 4478948 C T intron_variant MODIFIER c.1128+35C>T| S128
11 BAA05g08950 A05 4479849 G A stop_gained&splice_region_variant HIGH c.1334G>A|p.Trp445* S77
12 BAA05g08950 A05 4481046 G A synonymous_variant LOW c.1908G>A|p.Lys636Lys S45
13 BAA05g08950 A05 4482800 C T intron_variant MODIFIER c.2367+127C>T| S266
14 BAA05g08950 A05 4483262 C T synonymous_variant LOW c.2460C>T|p.Ser820Ser S10
15 BAA05g08950 A05 4483942 C T intron_variant MODIFIER c.2829+36C>T| S167
16 BAA05g08950 A05 4484322 G A intron_variant MODIFIER c.2830-304G>A| S302
17 BAA05g08950 A05 4484875 C T synonymous_variant LOW c.2982C>T|p.Leu994Leu S157
18 BAA05g08950 A05 4485326 G A missense_variant MODERATE c.3251G>A|p.Gly1084Glu S104
S52
19 BAA05g08950 A05 4486425 G A missense_variant MODERATE c.3704G>A|p.Gly1235Asp S6
20 BAA05g08950 A05 4487079 G A missense_variant MODERATE c.3904G>A|p.Glu1302Lys S138
21 BAA05g08950 A05 4487128 G A missense_variant MODERATE c.3953G>A|p.Gly1318Glu S64
22 BAA05g08950 A05 4487647 C T synonymous_variant LOW c.4146C>T|p.Arg1382Arg S162
23 BAA05g08950 A05 4487836 G A splice_region_variant&intron_variant LOW c.4202-4G>A| S226
24 BAA05g08950 A05 4487874 C T synonymous_variant LOW c.4236C>T|p.Thr1412Thr S19
25 BAA05g08950 A05 4488927 G A synonymous_variant LOW c.4659G>A|p.Thr1553Thr S124